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Because wavelength is an integral factor that contributes to responses evoked by UVR, we focused particularly on the wavelength dependence of NFAT responses.
To address whether oxidative stress contributes to responses to AA005, SW620 cells were treated with AA005 at 1 μM for 1 h, 4 h or 12 h, followed by incubation with fluorophore dichlorodihydrofluorescein diacetate (DCFDA), a dye to monitor intracellular ROS, for 30 min.
To address whether the oxidative stress contributes to responses of HCC and human immortal hepatic cells to adenanthin, all five liver cell lines were treated with adenanthin at 3 μM (for HepG2) or 9 μM (for other cells) for 1 h, followed by incubation with fluorophore dichlorodihydrofluorescein diacetate (DCFDA), a dye to monitor intracellular ROS, for 30 min.
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It is also possible that differences among major ion ratios within the general ion-matrix signature of Appalachian mine waters influence macroinvertebrate responses to TDS in a manner that contributes to response variability.
The difference in EOG amplitudes between wild type and eNOS-deficient mice argues that eNOS contributes to response adaptation.
We speculate that release of SE-S may contribute to responses to SE in vivo.
Th2 cells contribute to responses to parasites and many allergic diseases, but they represent a small fraction of CD4+ effectors during respiratory viral infections.
Salicylic acid (SA), jasmonate (JA), and ethylene (ET) contribute to responses to biotic stresses by influencing various signalling pathways with complex networks of synergistic and antagonistic interactions [ 2].
These biases may contribute to response behaviour, reducing the strength of grammatical explanations.
We found that both reference frames substantially contribute to response times in this task.
These data suggest that enzymes involved in citalopram metabolism may contribute to response, at least in some extensive metabolizers.
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